Supplier Quality Manager
Manchester, NH · On-site
The Supplier Quality Manager is responsible for leading the Supplier Quality Engineering (SQE ... MDR, and other relevant regulatory standards. * Partner cross-functionally with Engineering ...
New
Supplier Quality Manager
Manchester, NH · On-site
The Supplier Quality Manager is responsible for leading the Supplier Quality Engineering (SQE ... MDR, and other relevant regulatory standards. * Partner cross-functionally with Engineering ...
New
Quality Assurance Manager
Itasca, IL · On-site
... and MDR/adverse event reporting processes. ● Strong understanding of medical device ... quality management software tools. Preferred Attributes ● Experience with Class II or III ...
Quick apply
Quality Assurance Manager
Itasca, IL · On-site
... and MDR/adverse event reporting processes. ● Strong understanding of medical device ... quality management software tools. Preferred Attributes ● Experience with Class II or III ...
Solid understanding of 21 CFR 820, ISO 13485, EU MDR, MDSAP. * Demonstrated ability to manage and ... Experience managing quality systems with ISO 13485 and FDA 21 CFR Part 820, MDSAP, and EU MDR ...
Solid understanding of 21 CFR 820, ISO 13485, EU MDR, MDSAP. * Demonstrated ability to manage and ... Experience managing quality systems with ISO 13485 and FDA 21 CFR Part 820, MDSAP, and EU MDR ...
Quality Assurance Manager
Itasca, IL · On-site
... and MDR/adverse event reporting processes. ● Strong understanding of medical device ... quality management software tools. Preferred Attributes ● Experience with Class II or III ...
Quick apply
Quality Assurance Manager
Itasca, IL · On-site
... and MDR/adverse event reporting processes. ● Strong understanding of medical device ... quality management software tools. Preferred Attributes ● Experience with Class II or III ...
Quality Assurance Manager
Itasca, IL · On-site
... and MDR/adverse event reporting processes. ● Strong understanding of medical device ... quality management software tools. Preferred Attributes ● Experience with Class II or III ...
Quick apply
Quality Assurance Manager
Itasca, IL · On-site
... and MDR/adverse event reporting processes. ● Strong understanding of medical device ... quality management software tools. Preferred Attributes ● Experience with Class II or III ...
Quality Assurance Manager
Itasca, IL · On-site
... and MDR/adverse event reporting processes. ● Strong understanding of medical device ... quality management software tools. Preferred Attributes ● Experience with Class II or III ...
Quick apply
Quality Assurance Manager
Itasca, IL · On-site
... and MDR/adverse event reporting processes. ● Strong understanding of medical device ... quality management software tools. Preferred Attributes ● Experience with Class II or III ...
... EU MDR, ANVISA, MHLW, and TGA). General Duties and Responsibilities : * Ensure the ongoing integrity, adequacy, and appropriateness of the Quality Management System and associated processes.
... EU MDR, ANVISA, MHLW, and TGA). General Duties and Responsibilities : * Ensure the ongoing integrity, adequacy, and appropriateness of the Quality Management System and associated processes.
Quality Engineering Manager
Allen, TX · On-site
... EU MDR, ANVISA, MHLW, and TGA). General Duties and Responsibilities : * Ensure the ongoing integrity, adequacy, and appropriateness of the Quality Management System and associated processes.
Quality Engineering Manager
Allen, TX · On-site
... EU MDR, ANVISA, MHLW, and TGA). General Duties and Responsibilities : * Ensure the ongoing integrity, adequacy, and appropriateness of the Quality Management System and associated processes.
We are looking for an experienced MDR Manager to lead our Security Operations team. The ideal ... Run QA on closed alerts and incidents, drive down false positives, and maintain the team's runbooks ...
We are looking for an experienced MDR Manager to lead our Security Operations team. The ideal ... Run QA on closed alerts and incidents, drive down false positives, and maintain the team's runbooks ...
Supplier Quality Manager
Charlotte, NC · On-site
Supplier Quality Manager Who We Are Essity is a global leader in health and hygiene headquartered ... MDR, GxPs; * Knowledge of modern tools and application in continuous improvement projects (Six ...
Supplier Quality Manager
Charlotte, NC · On-site
Supplier Quality Manager Who We Are Essity is a global leader in health and hygiene headquartered ... MDR, GxPs; * Knowledge of modern tools and application in continuous improvement projects (Six ...
Supplier Quality Manager
Charlotte, NC · On-site
... FDA QSRs, EU - MDR, GxPs; Knowledge of modern tools and application in continuous improvement ... Knowledge of AI applications in supplier quality management, such as predictive analytics for ...
Supplier Quality Manager
Charlotte, NC · On-site
... FDA QSRs, EU - MDR, GxPs; Knowledge of modern tools and application in continuous improvement ... Knowledge of AI applications in supplier quality management, such as predictive analytics for ...
Senior Manager, Quality System & Compliance
San Francisco, CA · Hybrid
$195K - $250K/yr
... MDR, and MDSAP. This role is a unique blend of strategic foresight and tactical leadership ... Quality Management System (QMS) Oversight * Manage holistic aspects of the QMS to ensure compliance ...
Senior Manager, Quality System & Compliance
San Francisco, CA · Hybrid
$195K - $250K/yr
... MDR, and MDSAP. This role is a unique blend of strategic foresight and tactical leadership ... Quality Management System (QMS) Oversight * Manage holistic aspects of the QMS to ensure compliance ...
We are looking for an experienced MDR Manager to lead our Security Operations team. The ideal ... Run QA on closed alerts and incidents, drive down false positives, and maintain the team's runbooks ...
We are looking for an experienced MDR Manager to lead our Security Operations team. The ideal ... Run QA on closed alerts and incidents, drive down false positives, and maintain the team's runbooks ...
Assoc MDR/Vigilance Spec
Moundsview, MN · On-site
... quality compliance. Key Responsibilities * Process and review MDR complaint records. * Support complaint handling and medical device surveillance. * Manage adverse event report intake, evaluation ...
Assoc MDR/Vigilance Spec
Moundsview, MN · On-site
... quality compliance. Key Responsibilities * Process and review MDR complaint records. * Support complaint handling and medical device surveillance. * Manage adverse event report intake, evaluation ...
Create a culture of quality ensuring compliance with QMS, FDA QSR, ISO, MDR, and international ... Collaborate with CAPAs, non-conformances, and risk management to focus on process improvement.
Create a culture of quality ensuring compliance with QMS, FDA QSR, ISO, MDR, and international ... Collaborate with CAPAs, non-conformances, and risk management to focus on process improvement.
Regulatory Compliance and MDR * Ensure compliance with applicable medical device regulations ... Supplier Quality Management * Establish and maintain supplier qualification, monitoring, re ...
Regulatory Compliance and MDR * Ensure compliance with applicable medical device regulations ... Supplier Quality Management * Establish and maintain supplier qualification, monitoring, re ...
Regulatory Compliance and MDR * Ensure compliance with applicable medical device regulations ... Supplier Quality Management * Establish and maintain supplier qualification, monitoring, re ...
Regulatory Compliance and MDR * Ensure compliance with applicable medical device regulations ... Supplier Quality Management * Establish and maintain supplier qualification, monitoring, re ...
MDR Manager
Miami, FL · On-site
We are looking for an experienced MDR Manager to lead our Security Operations team. The ideal ... Run QA on closed alerts and incidents, drive down false positives, and maintain the team's runbooks ...
MDR Manager
Miami, FL · On-site
We are looking for an experienced MDR Manager to lead our Security Operations team. The ideal ... Run QA on closed alerts and incidents, drive down false positives, and maintain the team's runbooks ...
Regulatory Compliance and MDR Ensure compliance with applicable medical device regulations ... Supplier Quality Management Establish and maintain supplier qualification, monitoring, re ...
Regulatory Compliance and MDR Ensure compliance with applicable medical device regulations ... Supplier Quality Management Establish and maintain supplier qualification, monitoring, re ...
Manager, Quality Engineering Department: Quality Employment Type: Full Time Location: Gainesville ... Ensure alignment with FDA, ISO 13485, MDSAP, EU MDR, and internal QMS; maintain audit readiness and ...
Manager, Quality Engineering Department: Quality Employment Type: Full Time Location: Gainesville ... Ensure alignment with FDA, ISO 13485, MDSAP, EU MDR, and internal QMS; maintain audit readiness and ...
Mdr Quality Manager information
See salary details
$38.5K - $47.6K
5% of jobs
$47.6K - $56.7K
3% of jobs
$56.7K - $65.8K
9% of jobs
$70.9K is the 25th percentile. Wages below this are outliers.
$65.8K - $74.9K
13% of jobs
$74.9K - $84K
14% of jobs
The median wage is $88.1K / yr.
$84K - $93K
13% of jobs
$93K - $102.1K
12% of jobs
$107.8K is the 75th percentile. Wages above this are outliers.
$102.1K - $111.2K
11% of jobs
$111.2K - $120.3K
9% of jobs
$120.3K - $129.4K
7% of jobs
$129.4K - $138.5K
4% of jobs
$38.5K
$91K
$138.5K
How much do mdr quality manager jobs pay per year?
As of Sep 11, 2026, the average yearly pay for mdr quality manager in the United States is $91,047.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,500.00 and $110,000.00 per year, depending on experience, location, and employer.
What are popular job titles related to Mdr Quality Manager jobs?
For Mdr Quality Manager jobs, the most frequently searched job titles are:
Supplier Quality Manager
Manchester, NH • On-site
Merrimack Manufacturing
• Industrial Machinery Manufacturing • 51 - 200 employees51 - 200 employees
Full-time
Posted 2 days ago
New
Job description
Company Overview:
Merrimack Manufacturing is a medical device manufacturer located in the Manchester Millyard. We are a growing manufacturing company that will play a crucial part in bringing innovative and life changing products to life.
Position Overview:
The Supplier Quality Manager is responsible for leading the Supplier Quality Engineering (SQE) function and serving as the management representative for supplier quality within an ISO 13485-regulated medical device organization. This role provides strategic and operational leadership for supplier qualification, supplier performance management, and supplier quality system compliance across both New Product Introduction (NPI) and sustaining manufacturing operations.
The Supplier Quality Manager ensures that the organization's supply base consistently meets applicable regulatory requirements, including ISO 13485, FDA 21 CFR Part 820 and customer-specific requirements. This role acts as the primary escalation point for supplier quality issues and is responsible for driving supplier performance, compliance, and continuous improvement across the supply chain.
This is a full-time, on-site leadership position requiring regular interaction with cross-functional teams, suppliers, and manufacturing operations to support business objectives and ensure effective supplier quality management.
Responsibilities:
This version is more concise, leadership-focused, and consistent with typical Supplier Quality Manager postings in the medical device and regulated manufacturing industries.
Qualifications and Skills:
Merrimack Manufacturing is a medical device manufacturer located in the Manchester Millyard. We are a growing manufacturing company that will play a crucial part in bringing innovative and life changing products to life.
Position Overview:
The Supplier Quality Manager is responsible for leading the Supplier Quality Engineering (SQE) function and serving as the management representative for supplier quality within an ISO 13485-regulated medical device organization. This role provides strategic and operational leadership for supplier qualification, supplier performance management, and supplier quality system compliance across both New Product Introduction (NPI) and sustaining manufacturing operations.
The Supplier Quality Manager ensures that the organization's supply base consistently meets applicable regulatory requirements, including ISO 13485, FDA 21 CFR Part 820 and customer-specific requirements. This role acts as the primary escalation point for supplier quality issues and is responsible for driving supplier performance, compliance, and continuous improvement across the supply chain.
This is a full-time, on-site leadership position requiring regular interaction with cross-functional teams, suppliers, and manufacturing operations to support business objectives and ensure effective supplier quality management.
Responsibilities:
- Lead and develop the Supplier Quality team, driving a culture of accountability, collaboration, and continuous improvement.
- Develop and execute supplier quality strategies to ensure compliance with business, customer, and regulatory requirements.
- Own supplier qualification, onboarding, and performance management processes, including supplier selection, audits, risk assessments, and approval activities.
- Establish and maintain supplier governance programs, including Approved Supplier Lists (ASL), supplier risk management, quality agreements, and performance scorecards.
- Drive supplier performance improvements through effective management of audits, SCAR/CAPA systems, root cause investigations, and continuous improvement initiatives.
- Serve as the escalation point for critical supplier quality, compliance, and supply continuity issues, ensuring timely resolution and risk mitigation.
- Lead Supplier Review Board (SRB) activities, including supplier performance reviews, risk assessments, escalation decisions, and action planning.
- Ensure supplier compliance with applicable quality system requirements, including ISO 13485, FDA, EU MDR, and other relevant regulatory standards.
- Partner cross-functionally with Engineering, Manufacturing, Supply Chain, Procurement, and Product Development to support supplier selection, product launches, design transfers, and lifecycle management.
- Provide supplier quality leadership for new product introductions (NPI), supplier changes, transfer activities, and business continuity planning.
- Develop, monitor, and report supplier quality metrics and KPIs to drive data-based decision making and organizational performance.
- Support customer audits, regulatory inspections, and quality system assessments related to supplier controls and supplier management processes.
This version is more concise, leadership-focused, and consistent with typical Supplier Quality Manager postings in the medical device and regulated manufacturing industries.
Qualifications and Skills:
- 7-10+ years of experience in Supplier Quality, Quality Engineering, Manufacturing Quality, or related roles within a regulated medical device or similarly controlled industry.
- 3+ years of leadership experience managing or leading SQE teams or supplier quality functions.
- Strong experience with supplier qualification, audits, and global supply chain quality management.
- Demonstrated experience supporting NPI, design transfer, and process validation activities with external suppliers.
- Strong knowledge of ISO 13485, FDA 21 CFR Part 820 and global regulatory requirements.
- Deep understanding of manufacturing processes, process validation, and supplier process controls.
- Experience with contract manufacturers and global supply chain structures.
- Knowledge of risk management tools (FMEA), CAPA systems, and statistical quality methods.
- Strong problem-solving and root cause analysis skills (e.g., 8D methodology).
- Proficiency with supplier performance metrics and quality analytics.
- Proven ability to lead and develop technical teams in a regulated environment.
- Strong decision-making and escalation management skills.
- Ability to influence cross-functional and external stakeholders at all organizational levels.
- Excellent communication, negotiation, and supplier relationship management skills.
- Strategic thinker with strong operational execution capability.
- Ability and willingness to travel domestically and internationally (approximately 20-30%) for supplier visits, audits, assessments, and escalations.
About Merrimack Manufacturing
Sourced by ZipRecruiter
Industry
Industrial machinery manufacturing
Company size
51 - 200 Employees
Headquarters location
Manchester, NH, US